Rusty-patched bumble bee (Bombus affinis): COSEWIC assessment and status report 2010
Table of Contents
- COSEWIC Assessment Summary
- COSEWIC Executive Summary
- Species Information
- Name and classification
- Morphological description
- Genetic description
- Global range
- Canadian range
- Habitat requirements
- Habitat trends
- Habitat protection/ownership
- Life cycle and reproduction
- Natural Enemies
- Interspecific interactions
- Population Sizes and Trends
- Search effort
- Fluctuations and trends
- Rescue effect
- Limiting Factors and Threats
- Special Significance of the Species
- Existing Protection or Other Status Designations
- Technical Summary
- Acknowledgements and Authorities Consulted
- Information Sources
- Biographical Summary of Report Writer
- Collections Examined
List of Figures
- Figure 1. Photograph of female worker specimen collected at Pinery Provincial Park, Ontario, 2009
- Figure 2. Photograph of male specimen collected at Pinery Provincial Park, Ontario, 2005
- Figure 3. Photo of Bombus affinis queen (by S. Colla, York University). Specimen collected in 1971 at 1000 islands, Ontario
- Figure 4. Historic distribution of Bombus affinis
- Figure 5. Historical (prior to 2000) (triangles) and additional (circles) sites sampled during the summer of 2006 for the presence or absence of Bombus affinis throughout its eastern US range
- Figure 6. Bombus affinis records from 1899 – 2000 [includes databased specimens from examined collections, the Canadian National Collection online records and Milliron (1971)]. In Quebec the species has been confirmed from Gatineau and Montreal
- Figure 7. Sites surveyed for Bombus affinis by S. Colla
- Figure 8. Comparison of the relative abundance of each bumble bee species collected in Southern Ontario from 1971–1973
List of Appendices
Rusty–patched Bumble Bee
Endangered – 2010
COSEWIC -- Committee on the Status of Endangered Wildlife in Canada
COSEWIC status reports are working documents used in assigning the status of wildlife species suspected of being at risk. This report may be cited as follows:
COSEWIC. 2010. COSEWIC assessment and status report on the Rusty–patched Bumble Bee Bombus affinis in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. vi + 34 pp.
COSEWIC would like to acknowledge Sheila R. Colla for writing the status report on the Rusty–patched Bumble Bee Bombus affinis in Canada, prepared under contract with Environment Canada. This report was overseen and edited by Laurence Packer, Co–chair of the COSEWIC Arthropods Species Specialist Subcommittee.
For additional copies contact:
c/o Canadian Wildlife Service
Également disponible en français sous le titre Évaluation et Rapport de situation du COSEPAC sur le bourdon à tache rousse (Bombus affinis) au Canada.
Rusty–patched Bumble Bee -- Illustration by Elaine Evans.
© Her Majesty the Queen in Right of Canada, 2010.
Assessment Summary – April 2010
Rusty–patched Bumble Bee
Reason for designation
This species, which has a distinctive colour pattern, was once commonly found throughout southern Ontario. Active searches throughout its Canadian range have detected only one small population over the past seven years which suggests a decline of at least 99% over the past 30 years. It is threatened by disease, pesticides, and habitat fragmentation, each of which could cause extirpation in the near future.
Designated Endangered in April 2010.
Rusty–patched Bumble Bee Bombus affinis
The Rusty–patched Bumble Bee (bourdon à tache rousse) (Bombus affinis) is one of five North American members of the subgenus Bombus. It is a medium to large–sized bumble bee with several distinguishing characters. Males and workers have a second abdominal segment that is half reddish–brown and half yellow. Queens can be difficult to distinguish from some other species.
This species ranges from southern Ontario and southwestern Quebec in the north, south to Georgia and west to the Dakotas. In the southern parts of its range it occurs primarily at high elevations.
The Rusty–patched Bumble Bee has been recorded from diverse habitats including mixed farmland, sand dunes, marshes, urban and wooded areas. It has been recorded feeding from a variety of plant genera for pollen and nectar. It usually nests underground in abandoned rodent burrows.
This species, like all bumble bees, has an annual life cycle. Mated queens emerge from diapause in the spring and look for potential nest sites. The queen then forages and lays eggs to produce a brood of workers. Workers hatch and take over nest care and foraging. Towards late summer, males and new queens are produced. These reproductive individuals leave the colony and mate. Mated new queens go into hibernation while all other castes perish. Like other bumble bees, Rusty–patched Bumble Bee individuals have warning colouration and females will sting when touched.
Population sizes and trends
In the 1970s, the Rusty–patched Bumble Bee was relatively common compared to other bumble bee species. Dramatic declines were noticed by the mid–1990s in Canada and in the USA. In Canada, only three specimens were observed (one in 2005 and two in 2009) despite extensive targeted searches from 2005–2009.
Limiting factors and threats
The reason for the sudden decline of this previously common species throughout its large range is unknown. It has been hypothesized that the species suffered from introduced diseases from managed bumble bees used for greenhouse pollination. Additionally, habitat loss and the widespread use of a new group of pesticides likely pose substantial threats.
Special significance of the species
The Rusty–patched Bumble Bee is in flight for a longer period than are most other Bumble Bees and it visits numerous plant genera in many habitat types. Thus, it is likely an important pollinator of both agricultural crops and native flowering plants. The loss of this species may result in increased vulnerability of native mammals, birds and other organisms which rely on pollinated plants for food and shelter. This species has also been used in the past for scientific study as it is easily reared in captivity and has become an important reference species for research in physiology and sociobiology.
The Rusty–patched Bumble Bee is listed on the Xerces Society’s red–list of pollinator insects as ‘Imperiled’. No practical or legal protection exists in Canada or the USA.
The Committee on the Status of Endangered Wildlife in Canada (COSEWIC) was created in 1977 as a result of a recommendation at the Federal–Provincial Wildlife Conference held in 1976. It arose from the need for a single, official, scientifically sound, national listing of wildlife species at risk. In 1978, COSEWIC designated its first species and produced its first list of Canadian species at risk. Species designated at meetings of the full committee are added to the list. On June 5, 2003, the Species at Risk Act (SARA) was proclaimed. SARA establishes COSEWIC as an advisory body ensuring that species will continue to be assessed under a rigorous and independent scientific process.
The Committee on the Status of Endangered Wildlife in Canada (COSEWIC) assesses the national status of wild species, subspecies, varieties, or other designatable units that are considered to be at risk in Canada. Designations are made on native species for the following taxonomic groups: mammals, birds, reptiles, amphibians, fishes, arthropods, molluscs, vascular plants, mosses, and lichens.
COSEWIC comprises members from each provincial and territorial government wildlife agency, four federal entities (Canadian Wildlife Service, Parks Canada Agency, Department of Fisheries and Oceans, and the Federal Biodiversity Information Partnership, chaired by the Canadian Museum of Nature), three non–government science members and the co–chairs of the species specialist subcommittees and the Aboriginal Traditional Knowledge subcommittee. The Committee meets to consider status reports on candidate species.
- Wildlife Species
A species, subspecies, variety, or geographically or genetically distinct population of animal, plant or other organism, other than a bacterium or virus, that is wild by nature and is either native to Canada or has extended its range into Canada without human intervention and has been present in Canada for at least 50 years.
- Extinct (X)
A wildlife species that no longer exists.
- Extirpated (XT)
A wildlife species no longer existing in the wild in Canada, but occurring elsewhere.
- Endangered (E)
A wildlife species facing imminent extirpation or extinction.
- Threatened (T)
A wildlife species likely to become endangered if limiting factors are not reversed.
- Special Concern (SC)*
A wildlife species that may become a threatened or an endangered species because of a combination of biological characteristics and identified threats.
- Not at Risk (NAR)**
A wildlife species that has been evaluated and found to be not at risk of extinction given the current circumstances.
- Data Deficient (DD)***
- A category that applies when the available information is insufficient (a) to resolve a species’ eligibility for assessment or (b) to permit an assessment of the species’ risk of extinction.
* Formerly described as “Vulnerable” from 1990 to 1999, or “Rare” prior to 1990.
** Formerly described as “Not In Any Category”, or “No Designation Required.”
*** Formerly described as “Indeterminate” from 1994 to 1999 or “ISIBD” (insufficient scientific information on which to base a designation) prior to 1994. Definition of the (DD) category revised in 2006.
The Canadian Wildlife Service, Environment Canada, provides full administrative and financial support to the COSEWIC Secretariat.
COSEWIC Status Report on the Rusty–patched Bumble Bee Bombus affinis in Canada – 2010
Bombus affinis Cresson (1863) is a member of the well–known and economically important family Apidae, which includes, among others, all bumble and honey bees. The genus Bombus Latreille 1802 (=Bumble Bees) includes approximately 250 species found primarily in temperate regions of North America, Central America, South America, Europe and Asia. In North America, five species belong to the subgenus Bombus sensu stricto Latreille (Bombus occidentalis, B. franklini (critically endangered, IUCN), B. terricola, B. affinis and B. moderatus).
Bombus affinis Cresson was first described by Cresson (1863). While the taxonomy of some bumble bee species is controversial, the status of B. affinis is not (Cameron et al. 2007).
The classification of this species is as follows:
- Phylum Arthropoda,
- Class Insecta,
- Subclass Pterygota,
- Order Hymenoptera,
- Suborder Apocrita,
- Infraorder Aculeata,
- Superfamily Apoidea,
- Family Apidae,
- Subfamily Apinae
- Genus Bombus,
- Subgenus Bombus
- Species B. affinis.
Common names include the Rusty–patched Bumble Bee, Rusty–Tinged Bumble Bee and Affable Bumble Bee. In French it is called bourdon à tache rousse.
Workers and males are medium–sized (1–1.6 cm in length) with variable abdominal colouration ranging from T1 and T2 segments (the first of which is actually fused to the thorax and the second of which is the first segment of the apparent abdomen called tergum 1, or T1) all brown to T1 being yellow and T2 half brown and half yellow (Laverty and Harder 1988) with the latter combination being the most common (Figures 1 and 2). Queens are large (~2 cm in length) with yellow pile on the thorax and first two abdominal terga (Figure 3). The remaining abdominal segments are completely black. Near Boston, Mass., U.S.A., another colour morph (var. novae–angliae) has been described where males and workers have reddish pile on the third, fourth, fifth or sixth segments as well (Bequaert 1920). For all castes, the pile on top of the head and on the face is black, and on the thorax mostly yellow, except for the presence of black pile between the wing bases. None of the other members of this subgenus has these colour patterns. In all castes, the head is broadly rounded with the space between the base of the mandible and the compound eye about 2/3 as long as wide in queens and workers, and slightly wider than long in males (Laverty and Harder 1988). Relative to other bumble bee species, all castes of this species have a short tongue length (Laverty and Harder 1988).
Figure 1. Photograph of female worker specimen collected at Pinery Provincial Park, Ontario, 2009 (Photo by S. Colla, York University). No good quality images of living Canadian specimens are known for any sex or caste.
Figure 3. Photo of Bombus affinis queen (by S. Colla, York University). Specimen collected in 1971 at 1000 islands, Ontario. Note the lack of brown colouration on the second abdominal segment unlike the worker and male.
There have been no studies of the genetic structure of Bombus affinis populations. Cameron et al. (2007) used a specimen of B. affinis from Illinois for their comprehensive phylogeny of bumble bees. A male specimen collected at Pinery Provincial Park in 2005 was sequenced and submitted to the Barcode of Life Data Systems; the sequence will be available shortly on GenBank.
Bombus affinis is a haplodiploid organism with complementary sex determination (see Limiting Factors for further discussion with regards to this genetic system and extinction risk).
There is no reason to consider this species as representing more than one designatable unit.
Bombus affinis has been recorded across Eastern North America from the Dakotas in the west, to Ontario and Quebec in the north and south to Georgia (Figure 4; Milliron 1971).
Figure 4. Historic distribution of Bombus affinis. Map is based on A Monograph of the Western Hemisphere Bumblebees by Milliron (1971) as presented in Evans et al. (2008). Note that in the southern portion of the species’ range it occurs only at high altitudes.
During the summers of 2005–2007, 25 sites were surveyed for B. affinis throughout its U.S. range (Colla and Packer 2008). Seventeen of these sites were chosen based on previous records of B. affinis in various insect collections. Other sites were chosen within the species’ historic range. Using randomization software (Zayed and Grixti 2005), it was determined that by collecting 150 individual bumble bees at each site, there would be a less than 5% chance of missing B. affinis if it was present at historical abundances. To increase the chances of detection, 200 individuals were collected, identified and released at each site and the presence/absence of the species determined. Not a single B. affinis was collected at any of the surveyed sites (Fig. 5).
Figure 5. Historical (prior to 2000) (triangles) and additional (circles) sites sampled during the summer of 2006 for the presence or absence of Bombus affinis throughout its eastern U.S. range. No individuals of this species were found (from Colla and Packer 2008).
In the Bumble Bees of Eastern Canada (Laverty and Harder 1988), the species’ range in Canada is stated to be restricted to southern Ontario and southwestern Quebec. The collections surveyed for that publication and for this report did not yield a single specimen from any province other than QC and ON. In ‘Bees of the Eastern United States’ (Mitchell, 1962), it is stated that Bombus affinis occurs in three Canadian provinces (ON, QC, NB). The collection at Cornell University has specimens of B. affinis from New Brunswick county in New Jersey. This is likely an error and in the absence of any confirmed specimens from the Maritimes, it is assumed for this report that the range published in Laverty and Harder (1988) is correct. Figures 6 and 7 show southern Ontario divided into 100 x 100 km grid cells. Fifteen grid cells where B. affinis had been recorded historically (Fig. 6) were searched in 2005–2008. Previous studies have used grid cells to document range decline in bumble bees (Williams 1982; Fitzpatrick et al. 2007). During the recent survey, B. affinis occurred only in one grid cell at Pinery Park, in 2005, and was not seen there from 2006–2008 despite directed searches (see Search Effort). Two individuals were found in the park in August 2009. Additional sites (not included in Fig. 6) where the species has been collected in Quebec (historically in the late 1970s) include Longueuil, Saint–Pie, Granby, Saint–Hyacinthe (la Collection André–Francoeur à Saguenay, M. Savard, pers. comm.), but these specimens have not been verified by the report writer.
Figure 6. Bombus affinis records from 1899 to 2000 [includes databased specimens from examined collections, the Canadian National Collection online records and Milliron (1971)]. In Quebec the species has been confirmed from Gatineau and Montréal. Figure divided into 100 x 100 km grid cells. See Appendix 2 for list of numbered sites.
Symbols: Urban garden Urban Park Agricultural field Sand dune/Beach Marsh/Bog Forest Old Field/Meadow
For the purposes of this report, the historical Canadian range for this species does not include New Brunswick despite the distribution data suggested by Mitchell (1962). There are numerous reasons for excluding this province. Steve Javorek (Agriculture and Agri–Food Canada) recently compiled bumble bee community data from the Maritime Provinces from the past 15 years and did not come across a single Bombus affinis specimen (Javorek pers. comm. Nov. 2008). None of the collections examined for this report, including the Canadian National Collection, had any specimens from New Brunswick (Fig. 6). Sites were surveyed in June 2008 by S. Colla in southern and central New Brunswick for the purposes of this report, without any specimens of the species being detected. These sites were: Fredericton, Alma, Bay of Fundy National Park, Hopewell Cape, and Moncton. Entomologist Dr. Paul Williams of the Natural History Museum in London, England is the world authority on bumble bees and he does not have any records of B. affinis northeast of Maine (Williams pers. comm. Nov. 2008). Lastly, there are numerous studies published on the historical range of B. affinis which include only ON and QC in Canada (Milliron 1971; Laverty and Harder 1988; Evans et al. 2008). In conclusion, Mitchell (1962) likely gave the province of New Brunswick in error and the specimens he was referring to are likely from New Brunswick county in New Jersey, USA.
Bombus affinis is a generalist species. It requires a temperate climate and is restricted to regions south of the boreal forest. Compared to some other bumble bees, B. affinis seems to be relatively cold–tolerant and has been found at elevations as high as 1676 m in the southern parts of its range (Canadian National Collection).
Based on records from the U.S. and Canada, over 90% of B. affinis nests have been found underground, usually in old rodent burrows (Macfarlane 1974; Laverty and Harder 1988). Occasionally, B. affinis nests are found above ground, in one incidence inside an abandoned armchair (Macfarlane 1974). Nests of this species are likely similar to other bumble bee species but are extremely difficult to locate in the wild (Harder 1986). Brood cells and honey pots are made of wax produced by the queen and workers.
This species has been found foraging in a wide variety of habitats such as mixed farmland, sand dunes, marshes, urban and wooded areas.As the species is active from April to October a lengthy period of abundant flowering plants is required. Please see Appendix 1 for a list of recorded forage plant species.
There are no data on overwintering habitat for B. affinis but mated queens likely burrow underground, or in rotting logs as do queens of other Bombus species (Macfarlane 1974).
The majority of the species’ Canadian range occurs in southern Ontario with the remainder found in extreme SW Quebec. Southern Ontario is the most densely populated region in Canada and thus has much urban sprawl. Southern Ontario and Quebec also have a large percentage of land used for intensive agriculture. Globally intensive agriculture has shifted to relying on chemical fertilizers rather than traditional nitrogen–fixing plants (Matson et al. 1997). Nitrogen–fixing plants (e.g., clovers, alfalfa etc.) are rich in pollen and nectar and likely provide important forage habitat in agricultural areas. In the U.K., bumble bee declines have been attributed to the increasing lack of available forage in agricultural landscapes (e.g., Williams 1986; Goulson et al. 2005). Habitat trends specifically relating to this species in Canada are unknown.
Several suitable areas of B. affinis habitat are within protected areas. The most recently collected specimen was found in Pinery Provincial Park in Ontario, Canada. In the U.S., bumble bees have been surveyed in the past 10 years at Patuxent National Wildlife Refuge in Maryland by Sam Droege, and the Great Smoky Mountains National Park by Adrian Mayor. Specimens of this species have not been collected in either protected area since 2002 and 2000 respectively (Evans et al. 2008).
The following information is compiled from various references on general bumble bee biology (Alford, 1975; Laverty and Harder 1988; Goulson 2003; Benton 2006). Where applicable, references are provided for information pertaining to B. affinis specifically.
Bombus affinis is a typical primitively eusocial (i.e., it has queen and worker castes where the workers are the offspring of the queen) bumble bee with annual colonies (i.e., one year = one generation). Mated queens emerge from hibernation in the spring after overwintering and begin feeding. Spring queens search for a suitable nest site where they then begin their colonies. A few weeks after the queen’s initial egg–laying, female workers emerge and begin foraging for the colony and feeding the brood. As the summer progresses, the colony reaches maximum worker production and begins producing males and potential queens. These reproductive individuals leave the nest and mate. After mating, young queens enter diapause and overwinter. The males and the rest of the colony decline as fall approaches until they die in the winter. The largest colony recorded produced 2,100 individuals in captivity (MacFarlane 1974) but in the wild, colonies are likely much smaller. Very little is known about mating behaviour and colony dynamics in B. affinis. In a closely–related species, B. terrestris, females mate with a single male during a single mating event and the sperm is stored in a spermatheca until used in fertilization (Greeff and Schmid–Hempel 2008).
Eggs hatch after approximately four days and the small larvae begins to feed on pollen and nectar. The larval stage of bumble bees has four instars. After almost two weeks of development, the larvae spin cocoons and pupate. Pupae develop for another two weeks before hatching as full–sized adults. In total, development takes approximately five weeks but this varies with temperature and food supply (Alford 1975). Bombus affinis is a ‘pollen–storer’ meaning the larvae live in cells and are fed individually by adults opening the brood clump as the larvae develop. ‘Pollen–storing’ adults emerge relatively equal in size compared to ‘pocket–making’ bumble bee species, in which workers vary greatly in size due to unequal food distribution within the brood clumps.
Bombus affinis is one of the earliest bees to emerge in the spring and one of the latest to cease foraging in the fall (Lui 1973; Macfarlane 1974). According to data obtained from museum specimens (see collections examined), queens emerge sometime after mid–April and can continue to forage until the end of July. Workers have been collected foraging from mid–May until the end of September. In Guelph, ON, peak worker production was found to be during the middle two weeks of June (Lui 1973). Males have been collected from as early as mid–May to the end of October and new queens, from mid–August to late September (Lui 1973). The timing of the colony cycle can vary year to year with seasonal variation and latitude.
Like other sympatric bumble bees, B. affinis suffers from social parasites, where females enter the colony, kill the queen and lay eggs cared for by the remaining workers. Bombus (Psithyrus) ashtoni in particular specializes on usurping queens of B. affinis and the closely–related B. terricola. Bombus ashtoni is a naturally occurring social parasite which has not been seen anywhere for approximately 10 years, and is unlikely to have been a factor in the decline of B. affinis.
Microscopic endoparasites recorded infecting B. affinis include Sphaeruluria bombi (a nematode infecting 10% of overwintered queens) and Apicystis bombi (Neogregarinida: Ophrocystidae) (Macfarlane 1974; Macfarlane et al. 1995). Other parasites that are known to infect sympatric species are Nosema bombi (Microsporidia: Nosematidae) and Crithidia bombi (Kinetoplastea: Trypanosomatidae) (Colla et al.2006) but these have not been recorded in B. affinis (possibly because of their recent introduction from Europe and the rarity of B. affinis in recent years).
Macroparasites of sympatric species include conopid flies and Locustacarus buchneri (a tracheal mite) (Macfarlane et al. 1995). Predators include robber flies and crab spiders (S. Colla, pers. obs.). Raccoons, skunks and other mammals have also been known to eat bumble bee colonies (Breed et al. 2004).
Bumble bees have the rare physiological capability (among insects) to thermoregulate (Heinrich 2004). They are able to generate heat in their thoracic muscles, by shivering, to reach the required minimum temperature for flight (approx. 30°C) (Heinrich 2004). Given that bumble bees fly in the spring and fall in temperate regions, this internal temperature can be well above ambient temperature. Since B. affinis is one of the earliest spring emerging species, such thermoregulation is likely an extremely important adaptation.
There is no information specifically for B. affinis and little for bumble bees as a group on this subject. Nevertheless, given the patchiness of good quality bumble bee habitat (e.g., Hatfield and LeBuhn 2007) and increased problems associated with small effective population sizes in haplodiploid insects (Zayed and Packer 2005), dispersal is likely important to survival. The opportunity for dispersal occurs with the movement of reproductive individuals, primarily queens in spring that disperse while searching for suitable nest sites (Goulson 2003). There is some evidence that bumble bees are able to disperse relatively long distances. Males of a closely related species (B. terrestris) have been estimated to fly between 2.6 and 9.9 km from the colony of origin (Kraus et al. 2008). Additionally, B. terrestris was introduced to Tasmania in the early 1990s and has since spread at a rate of approximately 10 km per year (Stout and Goulson 2000). Passive dispersal of B. affinis by anthropogenic or other means is unlikely.
Because B. affinis is a generalist forager, it competes with many other bee species for food resources. In particular, because of similar tongue lengths, B. affinis likely competes for nectar with the introduced honey bee: Apis mellifera. However, competition is extremely difficult to study in natural conditions (Thomson 2006) and because honey bees have been in North America for hundreds of years, it is difficult to ascribe recent reductions in B. affinis to impacts of direct competition with honey bees.
Native bumble bees which may be possible competitors of B. affinis include B. impatiens, B. bimaculatus, B. rufocinctus, B. griseocollis. These species have short to medium tongue lengths and seem to have increased in abundance or range in recent decades (Colla and Packer 2008). Bombus impatiens in particularhas increased in numbers substantially in urban areas (Colla and Packer, in prep.), has expanded its range (Sheffield et al. 2003) and is increasingly managed for greenhouse and field crop pollination (e.g., Shipp et al. 1994).
Bombus affinis likely has important mutualisms with early spring flowering plant species which may rely on it for pollination. These plants are likely among those included in Appendix 1 but other, unrecorded host plant species, may also be negatively impacted by declines in B. affinis populations. The extent of interdependence of individual plant species with B. affinis is unknown.
The survival of B. affinis in spring and fall in temperate climates is aided by their relatively large body size and dense pile. Their physiological ability to thermoregulate to temperatures above ambient temperatures allows them to adapt to the colder climates at the northern edge of their range. Behavioural modifications (such as ceasing foraging mid–day in hot weather and fanning of the colony) also aid in temperature regulation.
The female stinging apparatus and warning colouration provide protection against some predators and humans.
Members of the subgenus Bombus have evolved a behavioural adaptation known as ‘nectar–robbing’. Although these members have relatively short tongues, they pierce the corollas of floral nectar tubes to access nectar from long–tubed flowers. They can thus obtain nectar in the absence of floral hosts to which their tongue length is more closely adapted.
Bombus affinis has been reared in captivity relatively easily in the past for scientific study (R. Gegear and the late T. Laverty pers. comm., Macfarlane 1974).
Compared to most other insects, bumble bees are quite easily found and identified in the field. As a result, many studies have investigated various ecological and evolutionary mechanisms using Bombus as a model system, resulting in the documentation of the presence of B. affinis in various regions of the U.S. and Canada. Southern Ontario in particular has been the region where many studies of bumble bee ecology have been performed (e.g., Macfarlane 1975). However, until recently, very few surveys have been conducted to specifically determine the status of the species in the wild and to document changes in populations from year to year.
Colla and Packer (unpublished data) surveyed sites throughout southern Ontario to determine whether there have been changes in bumble bee communities over time compared to historical data (Fig. 7). Sites were surveyed in the summers from 2005–2008 for a minimum of 1 day but in some cases individual sites were surveyed for multiple days and years. More details on the sampling protocol can be found in Colla and Packer (2008). Despite sampling throughout the native Canadian range for B. affinis, only one specimen was found (Fig. 2). A male was collected in Pinery Provincial Park in August 2005. Each summer from 2006–2008, the park was surveyed for bees every 10 days from May to September and B. affinis individuals were not observed (A. Taylor, pers. comm.). S. Colla searched the park specifically for B. affinis for 2 days in August (when colonies are expected to be at their peak) each year from 2005–2009. From 2006–2008, not a single B. affinis individual was found. On August 21st 2009, two workers were found in the park, one on Spotted Knapweed and the other in a pan trap.
In total, over 600 hours of targeted search have been made for this species in Ontario since 2004 and thousands of hours of general bee survey work have been performed in areas previously inhabited by the species.
Population sizes for Ontario and Quebec are unknown. In the past 10 years only three individuals have been collected in Canada despite active searching at historical sites.
Colla and Packer (2008) documented the decline in relative abundance of B. affinis after a 30–year period. Sites in Guelph and Belwood, Ontario were surveyed for bumble bees for three years (2004–2006) and the data compared to those from surveys performed in 1971–1973 at the same sites (Macfarlane 1974). In both studies, bumble bees were opportunistically collected using insect nets and identified to species. The studies differed in sampling intensity with Macfarlane (1974) sampling approximately every few days and Colla and Packer sampling once a week in 2006 and less frequently in 2004 and 2005. The study from 1971–1973 found that approximately 14% of the 3632 bumble bees collected were B. affinis making it the 3rd–4th most abundant bumble bee species. Using randomization software, it was determined that in order to detect B. affinis at the levels present in Macfarlane (1974), 150 bumble bees should be sampled at each site (at P<0.05 the chance of missing the species, if it was there, was less than 5%) (Colla and Packer 2008). From 2004–2006, a total of 1195 bumble bees were collected in the same sites (Speed River, Guelph and near Belwood Lake), none were B. affinis. This was the most dramatic decline of all the bumble bee species in the region (Fig. 8).
Figure 8. Comparison of the relative abundance of each bumble bee species collected in Southern Ontario from 1971–1973 (black) (Macfarlane 1974) and 2004–2006 (grey) (* indicates P < 0.001) (from Colla and Packer 2008).
There are difficulties associated with determining the abundance and/or effective population sizes of eusocial organisms. While abundance may be high at a given site, unless it is determined that all individuals are not from the same colony, the effective population size will be a tiny fraction of the number of individuals collected (Packer and Owen 2001; Darvill et al. 2004). The best measure of effective population size (in the absence of genetic data) is to survey queens (e.g., Kokuvo et al. 2008), but this may be detrimental to wild populations and difficult to accomplish as they are hard to find and emergence times differ from year to year.
Given the species’ previously wide distribution in southern Ontario and just across the border in Quebec, its reduction to a single known site would indicate a reduction in EO, IAO and population size of at least two orders of magnitude.
Surveys have been carried out throughout the U.S. and Canadian range of B. affinis to determine whether populations have suffered the declines noted anecdotally. In all cases where adequate baseline data exist, B. affinis populations have suffered substantial declines (Colla and Packer 2008; Evans et al. 2008; Giles and Ascher 2006; Grixti et al. 2009). In recent decades, Canadian occurrences have declined (three individuals seen despite extensive searching) (see under Canadian range) and thus populations appear to have declined to the same extent.
In the U.S., there is also evidence for a declining trend in this species. Recent bee surveys from New York state, where B. affinis was once ‘moderately abundant’ (Leonard 1928), yielded no individuals despite a combined total of over 1460 collected bumble bees (Giles and Ascher 2006; Matteson et al. 2008). Grixti et al. (2009) used an electronic database and recent survey results to determine changes in the distribution and composition of bumble bees throughout Illinois. Based on data from 56 sites from 1900–1999 and 2000–2007, B. affinis declined in distribution by 33%. Additionally, 90% of the 50 B. affinis specimens collected during the latter time period were obtained from a single site.
The rarity of this previously common species throughout its entire range in the U.S. (NRC 2007; Evans et al. 2008) would make recolonization of Canada highly unlikely. The only individuals documented in the U.S. in 2009 were in Daubenspeck Park, Indianapolis, Indiana, U.S.A. (Liz Day pers. comm.).
Bombus affinis is at the most northern edge of its range in southern Ontario and SW Quebec. It is not known whether there is a physiological, behavioural or geographical barrier limiting its dispersal northwards. Climatic variables such as snow cover, precipitation, growing season length, etc., are likely important determinants of suitable habitat for bumble bees. Given the restriction of B. affinis’ range to high elevations at the southern part of its range, it seems likely that this species is restricted to a narrow climatic niche. Williams et al. (2009) showed that bumble bees with narrow climatic niches are more vulnerable to extinction.
The rapid decline of B. affinis and other members of the subgenus Bombus s.str. seems to have commenced in the mid–1990s (NRC 2007). Bombus franklini, the species most closely related to B. affinis, has disappeared from its range in western USA and is listed by the IUCN as critically endangered (Evan et al. 2008). Bombus terricola and B. occidentalis have also declined throughout their ranges in Eastern and Western North America respectively (NRC 2007; Evans et al. 2008). These declines have not yet been attributed to any one cause, but based on the timing of the observed collapse, possible threats have been hypothesized (NRC 2007; Evans et al. 2008).
Pathogen spillover has been implicated in the significant declines of many animals (Morton et al. 2004; Power and Mitchell 2004) but is a poorly understood threat for bumble bees. Pathogen spillover occurs when pathogens spread from a heavily infected ‘reservoir’ host population to a sympatric ‘non–reservoir’ host population (Power and Mitchell 2004). The use of commercial bumble bees (Bombus impatiens in Canada) for greenhouse pollination with a high prevalence of parasites has been shown to cause pathogen spillover into populations of wild bumble bees foraging nearby (Colla et al. 2006; Otterstatter and Thomson 2008). Parasites found in commercial colonies have been found in species other than B. impatiens (Macfarlane 1974; Macfarlane et al. 1995; Colla et al. 2006) but the extent of their lethal and sublethal effects in other Bombus species remains unknown. Nonetheless, the increased use of bumble bees in greenhouse operations in recent decades has been implicated in the decline of members of the subgenus Bombus, including B. affinis and B. terricola (Thorp and Shepherd 2005; Berenbaum et al. 2007; Evans et al. 2008).
Around the time when the declines of B. affinis and other members of its subgenus were noted, a new pesticide (Imidacloprid, a neonicotinoid) was registered for use in the US and Canada (1994 and 1995 respectively: Cox 2001; PMRA 2001). Neonicotinoids have been shown to be especially lethal to bees (compared to other pesticides) even at concentrations in the parts per billion (ppb) range (EPA 1994; Marletto et al. 2003). Neonicotinoids are suspected of causing dramatic honey bee declines in Europe (resulting in their having been banned in some countries) and the U.S. (Schacker 2008; Williams 2008) and in having negative impacts on a bumble bee in the same subgenus as B. affinis (Tasei et al. 2001). The neonicotinoids are now commonly used in regions of eastern North America for crop, forest and turf pest control (Cox 2001). In Ontario, the amount of imidacloprid used in 2003 in agriculture was approximately 527 kg (McGee et al. 2004; Brimble et al. 2005). The total quantity of imidacloprid used in Ontario is likely considerably larger if pet flea control, tree root drenches, greenhouse and turfgrass uses are included. These pesticides are systemic and travel throughout the plant, reaching pollen and nectar (Sur and Stork 2003). Imidacloprid is non–lethal to bumble bees when used as directed (e.g., Tasei et al. 2001); however, studies of its effects on bumble bees only tested one species, B. impatiens, as the representative for all species in Eastern North America (Gels et al. 2002; Morandin and Winston 2003). The lethal and sub–lethal effects of this group of pesticides urgently need to be determined for a wider range of species. Various life history traits of B. affinis (such as large body size, early emergence, long colony cycle, etc.) may make it especially vulnerable to accumulation of pesticides in the colony. Large areas used for golf courses may expose bumble bees to large quantities of pesticides in otherwise good habitat (Tanner and Gange 2004). A recent meta–analysis of environmental impacts upon bees has demonstrated that eusocial species are disproportionately affected by pesticides (Williams et al., submitted).
Another suspected threat to Bombus affinis populations is habitat loss. As mentioned above, bumble bees are more vulnerable to habitat fragmentation than other animal species for genetic reasons (Packer and Owen 2001). They also require large inputs of resources over a long period of time (April – October for B. affinis) as reproductives for the next generation are only produced towards the end of the colony cycle. The increased reliance on intensive agriculture over the past few decades has resulted in decreased quality foraging habitat for bumble bees globally (e.g., Williams 1989; Kosior et al. 2007). Additionally, southern ON and QC contain some of the most highly populated/urbanized regions of Canada. Suitable nesting, hibernating and foraging habitat is possibly difficult to find in these regions and is likely in short supply. Habitat loss is a steady long–term threat to this species, and likely does not explain its sudden collapse.
Bumble bees are haplodiploid organisms with complementary sex determination which makes them extremely susceptible to extinction when effective population sizes are small (Zayed and Packer 2005). This is due to the ‘diploid male extinction vortex’ (Zayed and Packer 2005). Sex in bees, and most other haplodiploids, is determined by genotype at a single “sex locus”: hemizygotes (haploids) are males, heterozygotes are female and homozygotes are diploid males. Diploid males are usually sterile or inviable. The number of sex alleles in a population determines the proportion of diploids that are male and is itself determined primarily by the effective size of the population. This means that as bumble bee populations decrease in size, the frequency of diploid males increases. As diploid males are attempts at female production, their increasing production in smaller populations increases the rate of population decline causing a special case of the extinction vortex: “the diploid male extinction vortex.” This special form of genetic load is the largest known (Hedrick et al., 2006). In practical terms, if a bee population decreases to a few reproducing individuals, it is certain to become extinct even under stable environmental conditions unless its number increases within a few generations.
Bombus affinis is an important pollinator of native flowering plants and crops in North America. A thorough study of bumble bee floral host use indicated B. affinis visits at least 65 plant genera (Macfarlane 1974). In particular, it has been shown to be an excellent pollinator of cranberry (Cane and Schiffauer 2003), plum and apple (Medler and Carney 1963), alfalfa (Holm 1966), and onion (Caron et al. 1975). The long colony cycle of this species makes it likely to be the primary pollinator for many ecologically and economically important plants (including apple, raspberry, lilac, honeysuckle, hawthorn, nightshade, clover, milkweed, goldenrod and aster). Upon pollination, some of these plants provide fruits which sustain various avian and mammalian species among others. The loss of this bumble bee species may result in changes in food chains and ecosystem sustainability. Some of the noted visited plants for B. affinis also have important medicinal properties for First Nations people (e.g., Aralia, Rosa, Rubus, and Spiraea).
Bombus affinis is also ecologically important as it has one of the largest colony sizes ever recorded for a North American bumble bee species (Macfarlane 1974). Additionally, the social parasite bumble bee species B. ashtoni specializes on members of this subgenus (Laverty and Harder 1988), and has also suffered substantial declines in recent years (Evans et al. 2008) probably as a consequence of host declines.
Because Bombus affinis is relatively easily reared in captivity and was historically quite common, it was used as a model system for various physiological and ecological experiments (e.g., Macior 1966; Fisher 1983; Bregazzi and Laverty 1992; Schiestl and Barrows 1999) and it is thus an important reference species for experimental biology and research.
Bumble bees are of special significance to First Nations people. Symbolically bumble bees have been depicted on totem poles, ceremonial masks, in artwork and legends. However, there is no known specific cultural significance for B. affinis.
Xerces Society of Invertebrate Conservation Red List Status: ‘Imperiled’ = “At high risk of extinction due to very restricted range, very few populations (often 20 or fewer), steep declines, or other factors”. The Xerces Society is a nonprofit organization which performs research and advocates for insect conservation. As a result their red–list does not provide any legal protection for the listed insects.
Canada–Species at Risk Act: None
Canada–Provincial Status: Ontario Natural Heritage Information Centre (ONHIC) Rank: S1 Critically Imperiled
USA– Endangered Species Act: None
IUCN Red list: None
Rusty–patched Bumble Bee – bourdon à tache rousse
Range of occurrence in Canada (province/territory/ocean): Ontario, Quebec
is being used)
individuals over any 10 year period, over a time
period including both the past and the future.
Extent and Occupancy Information
of one known site.
(Always report 2x2 grid value; other values may also
be listed if they are clearly indicated (e.g., 1x1 grid, biological AO)). Based upon existence of one known site.
area of occupancy?
and quality of habitat?
* See definition of location.
Number of Mature Individuals (in each population)
Threats (actual or imminent, to populations or habitats)
The one remaining known site in Canada is in Pinery Provincial Park. If the main cause of decline is disease then the chances of disease spreading to the park is high. If the cause is pesticide use, then pesticide drift is possible and would likely impact the species at any time from April to September. Given the small size of the remnant population, the genetic load caused by the unusual sex determining mechanism in bees is likely to result in extinction unless numbers increase considerably very quickly.
Rescue Effect (immigration from outside Canada)
Michigan, SC; Wisconsin, SU.
Rare throughout range. On Xerces Society’s Red List for At–Risk pollinators
Status and Reasons for Designation
Reasons for designation:
This species, which has a distinctive colour pattern, was once commonly found throughout southern Ontario. Active searches throughout its Canadian range have detected only one small population over the past seven years which suggests a decline of at least 99% over the past 30 years. It is threatened by disease, pesticides, and habitat fragmentation, each of which could cause extirpation in the near future.
Applicability of Criteria
Criterion A (Decline in Total Number of Mature Individuals):
Meets Endangered A2ce. Both the abundance and area occupied have declined. The putative causes of decline (pathogens, pollutants, and fragmentation) have not ceased.
Criterion B (Small Distribution Range and Decline or Fluctuation):
Meets Endangered B1ab(i,ii,iv,v)+2ab(i,ii,iv,v). The EO and IAO are both 4 km², the species has been found only at one site since 2000 despite repeated searches for it throughout its previous Canadian range, and continuing decline in EO, IAO, number of locations and number of individuals is expected based upon any of the putative threats. Decline in habitat is also probable.
Criterion C (Small and Declining Number of Mature Individuals): Not applicable. The total number of individuals remains unknown, although is certainly very small and probably less than the 2,500 threshold for endangered but this cannot be stated with certainty.
Criterion D (Very Small or Restricted Total Population): Not applicable. Total population is unknown.
Criterion E (Quantitative Analysis): Not performed.
The report writer would like to thank Dr. Paul Williams, Dr. Laurence Packer and the Xerces Society for Invertebrate Conservation (particularly E. Evans and S. Jepsen) for valuable discussion and information. Thank you also to the various museum curators for allowing me to examine specimens, especially Steve Marshall at U. of Guelph and Ontario Parks for support during fieldwork. Funding was provided by Environment Canada. Survey work completed in southern Ontario was funded by an NSERC Discovery grant to Laurence Packer.
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Sheila R. Colla has studied various aspects of bumble bee ecology and behaviour throughout North America. Previously she worked as a research assistant to Dr. James Thomson, Dr. Michael Otterstatter, and Dr. Robert Gegear at the University of Toronto, St. George Campus looking at pathogen spillover from managed to wild bumble bee populations. She is currently a doctorate student and recipient of the NSERC Alexander Graham Bell Canadian Graduate Scholarship at York University, Toronto, ON under the supervision of Dr. Laurence Packer. Her dissertation examines changes in bumble bee communities over the past century and looks into some of the causes for observed declines. In addition, she is a member of the North American Pollinator Protection Campaign and her research has been featured in The Washington Post, Canadian Gardening, The Toronto Star, BioScience, CBC’s Quirks and Quarks, and The Daily Planet for Discovery Channel Canada.
The following collections were consulted and all contain specimens of Bombus affinis:
Canadian Museum of Nature, P.O. Box 3443, Stn. D, Ottawa, ON, Canada K1P 6P4
Canadian National Collection ‘Bombus of Canada Dataset’ [Online records] [Accessed December 2008]
Royal Ontario Museum, 100 Queen’s Park, Toronto, Ottawa, ON, Canada M5S 2G6
University of Guelph Insect Collection, 1216 Edmund C. Bovey Building, University of Guelph, Guelph, ON, N1G 2W1
York University Bee Collection, Dept. of Biology, 4700 Keele St. Toronto, ON M3J 1P3
Bombus affinis visits a wide variety of plants including Abelia grandiflora, Aesculus spp., Asclepias syriaca, A. incarnata, A. verticillata, Aralia spp., Aster spp., Aquilegia canadensis, Aureolaria pedicularia, Berberis spp., Camassia scilloides, Carduus sp., Ceanothus americanus, Cercis canadensis, Chamaedaphne calyculata, Coreopsis major, Crataegus spp., Delphinium tricorne, Dicentra canadensis, D. cucullaria, Echium vulgare, Helianthus spp., Hydrangea spp., Hydrophyllum spp., Impatiens capensis, Lamium purpureum, Laportea spp., Leonurus sp., Linaria sp., Lonicera spp., Lotus corniculatus, Medicago sativa, Mertensia virginica, Monarda sp., Nepeta spp., Pedicularis canadensis, Pedicularis lanceolata, Philadelphus spp., Polymnia spp., Prunella vulgaris, Prunus spp., Pyrus ioensis, Pyrus malus, Rhododendron spp., Rhus spp., Ribes spp., Robinia spp., Rosa spp., Rubus spp., Salix spp., Solanum sp., Solidago spp., Symphytum officinale, Syringia spp., Syringia vulgaris , Taraxacum spp., Trifolium spp., Vaccinium spp., Verbascum spp., Verbesina occidentalis, Vicia spp.
Additional food plant genera records published in Milliron (1971) are: Angelica, Aster, Cirsium, Epilobium, Eupatorium, Lythrum, Malus, Spiraea, Veronica, Parnassia, Hypericum, Kalmia and Rosa.
Appendix 2. Sites where Bombus affinis was found historically in Canada (Figure 6)
- Bright’s Grove
- Chaffey’s Locks
- Forks of the Credit
- Gatineau Provincial Park
- Pinery Provincial Park
- Lake Matchedash
- Manester Tract, St. Williams
- Miller Lake
- Mt. Hope
- Niagara Glen
- Ojibway Prairie
- Oliver Bog
- Owen Sound
- Pelee Island
- Pike Bay
- Grand Bend
- Pork Hill
- Port Dover
- Port Franks
- Port Hope
- Port Ryerse
- Puslinch Lake
- Rock Dunder, Morton
- S. March
- St. David’s
- St. John’s west
- Vineland Station
- Wasaga Beach
- Woodbridge, Boyd Conservation Area
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